113850-15-0

Basic information

• Product Name: Dansyl-isopropylaMine
• Synonyms: Dansyl-isopropylaMine
• CAS NO: 113850-15-0
• Molecular Formula: C15H20N2O2S
• Molecular Weight: 292.3965
• Product Categories: Amines, Aromatics, Fluorescent Labels & Indicators, Sulfur & Selenium Compounds
• Mol File: 113850-15-0.mol

Chemical Properties

• Boiling Point: 431.9±37.0 °C(Predicted)
• Appearance: /
• Density: 1.190±0.06 g/cm3(Predicted)
• Storage Temp.: Hygroscopic, Refrigerator, Under Inert Atmosphere
• Solubility: Chloroform, Ethyl Acetate
• PKA: 12.24±0.50(Predicted)
• CAS DataBase Reference: Dansyl-isopropylaMine(CAS DataBase Reference)
• NIST Chemistry Reference: Dansyl-isopropylaMine(113850-15-0)
• EPA Substance Registry System: Dansyl-isopropylaMine(113850-15-0)

Safety Data

• Hazardous Substances Data: 113850-15-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agricultural Industries:
Dansyl-isopropylamine is used as a key intermediate for the synthesis of pharmaceutical and agricultural goods. Its application reason is due to its ability to be incorporated into the chemical structure of various products, enhancing their effectiveness and performance.
Used in Glyphosphate Herbicide Production:
Dansyl-isopropylamine is used as a crucial component in the production of glyphosphate herbicides. It contributes to the herbicidal activity by being an integral part of the chemical structure, which aids in the effective control of weeds and unwanted plant growth.
Used as an Additive in the Petroleum Industry:
Dansyl-isopropylamine is also used as an additive in the petroleum industry. Its application reason is to improve the properties of fuels and lubricants, such as enhancing their stability, reducing wear, and providing better overall performance.

Upstream product

• 605-65-2 5-(dimethylamino)naphth-1-ylsulfonyl chloride 
• 75-31-0 isopropylamine 

Relevant articles and documents

Collisional reaction of liquid droplets: Amidation of dansyl chloride observed by fluorescence enhancement

The collisional reaction of droplets is observed by time-resolved fluorescence spectroscopy. Colliding droplets of the reactant solutions are irradiated with a pulsed laser, and the resulting fluorescence spectra and images of the colliding droplets are observed as a function of the elapsed time from the collision. The amidation reaction of dansyl chloride with isopropylamine is observed through fluorescence enhancement on a microsecond time scale. The present method enables us to measure the early stages of reactions in solutions.

Functionalization of α-C(sp3)?H Bonds in Amides Using Radical Translocating Arylating Groups

α-C?H arylation of N-alkylamides using 2-iodoarylsulfonyl radical translocating arylating (RTA) groups is reported. The method allows the construction of α-quaternary carbon centers in amides. Various mono- and disubstituted RTA-groups are applied to the arylation of primary, secondary, and tertiary α-C(sp3)?H-bonds. These radical transformations proceed in good to excellent yields and the cascades comprise a 1,6-hydrogen atom transfer, followed by a 1,4-aryl migration with subsequent SO2 extrusion.

Combinatorial dansyl library and its applications to pH-responsive probes

Herein, we report the first 48-membered, dansyl-based, combinatorial fluorescent library. From the electronic and structural properties of the probes, we analyzed their optical properties and chemical yields, with an average of 49 %. The molecules were ex